Antimicrobial packaging system

ABSTRACT

Implementations of the present invention extend to sanitary systems, methods, and devices configured to package food items with an even coating of an accurate amount of sanitizing agent, such as an antimicrobial agent. In one implementation, an exemplary system comprises a combination of air nozzles, anti-bacterial spray nozzles or spray headers, metering valves, and timers to achieve uniform distribution of an antimicrobial solution into a product package, and subsequently provide a uniform distribution of the antimicrobial solution to the food item.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present invention is a Continuation Application of U.S. NationalStage application Ser. No. 12/918,304, filed on Aug. 18, 2010, entitled“Antimicrobial Packaging System,” which corresponds to PCT ApplicationNo. PCT/US10/45578, filed on Aug. 16, 2010, which claims priority toU.S. Provisional Patent Application No. 61/243,830, filed on Sep. 18,2009. The entire contents of each of the afore-mentioned patentapplications are hereby incorporated by reference in their entirety.

BACKGROUND OF THE INVENTION

1. Technical Field

The present disclosure represents devices, systems and methods forsanitary packaging of food items.

2. Background and Relevant Art

Recently, the United States Department of Agriculture (USDA) expandedits interpretation of products subject to recall in the event of apathogenic contamination event. Prior to this time, a recall event inraw or ground beef trimmings would be limited to just those trimmingsand grinds produced at the same time the contaminated product was alsobeing produced. For example, the product that would be affected underthe prior USDA interpretation would include only those trimmings andgrinds produced between one complete sanitation event, and the nextcomplete sanitation event, with no trimmings or grinds being allowed tocarry over from one sanitation period to the next.

More recently, and with the USDA's expanded interpretation, the productssubject to recall would include not only trimmings and grinds, but alsoall primal cuts (whole muscle cuts). This expansion in interpretationgreatly increases the costs, and therefore, increases the loss inprofits that may be associated with a recall event.

Under the current USDA interpretation, there is a consideration that maygive meat producers the ability to use additional microbialinterventions on primal cuts as a further process step that woulddifferentiate primal cuts from trim and ground beef in an event of arecall: apply a scientifically proven pathogen reduction processuniformly to all beef primal cuts immediately prior to packaging. Inorder to satisfy the USDA standards for this consideration, a meatproducer must demonstrate that the pathogen reduction process doesindeed uniformly apply an accurate amount of an antimicrobial agent tothe primal cuts immediately prior to packaging.

There are several conventional antimicrobial agents that have beendocumented and acknowledged by the USDA as providing the necessarypathogen reduction step. Some antimicrobial agents that have beenacknowledged include lactic acid, peracetic acid, ammonia hydroxide, andchlorine dioxide/sodium hypochlorite.

Although several antimicrobial agents may have been approved, theapplication of the antimicrobial agent to the primal cuts presentsvarious challenges. A primary difficulty in the application processdeals with obtaining complete product coverage, i.e., coverage on allsurfaces of the primal cut. A second concern is that the antimicrobialagent must be applied at a carefully metered rate so that any individualprimal cut does not gain more than 0.49% by weight with the addition ofthe antimicrobial solution (another USDA requirement). Additionally,application of a antimicrobial agent that provides full coverage andaccurate amounts may be cost prohibitive and subject to human error inproduct handling and application rate.

For example, conventional methods of applying an antimicrobial agent mayemploy multiple spray nozzles that aim at all sides of the product as itpasses along a moving conveyor. The conventional method may employ asplit in the conveyor, or a transition between two consecutiveconveyors, to spray the underside of the primal cut. Frequently,however, multiple primal cuts may enter the spraying area simultaneouslyand may be touching, overlapping, or otherwise obstructing the spraynozzles ability to coat all surfaces of any given piece of product.Therefore, such an application method requires constant oversight toensure proper pacing, spacing, and antimicrobial solution coverage,which in turn increases costs and decreases efficiency.

Other conventional methods may also have difficulty applying the correctamount of the antimicrobial agent, thus causing the weight of the foodproduct to increase over the USDA standard set at 0.49%. For example, ina typical method that employs several spray nozzles, it is may bedifficult to meter the actual amount of antimicrobial solution that isapplied to an individual piece of product. For instance, although theamount of antimicrobial solution may be metered through a spray nozzle,many times there is over-spray and/or under-spray that unpredictablyaffects the total amount of antimicrobial solution deposited on thepiece of product. Thus, in many conventional processes, it is difficultto apply the correct amount of antimicrobial solution.

Moreover, in an effort to provide an even application and correct amountof antimicrobial agent, other convention methods may use labor intensiveprocesses that increase the cost of packaging the meat, and decrease theefficiency of the packaging process. For example, some conventionalprocesses employ workers that individually apply the antimicrobialsolution to each piece of product. This process, however, may be timeconsuming, produce non-uniform results, and be rather expensive whencompared to automated processes. Accordingly, there are a number ofdisadvantages in the conventional art of sanitary packaging of fooditems.

BRIEF SUMMARY OF THE INVENTION

Implementations of the present invention systems, methods and apparatusconfigured to package food items with an even coating of anantimicrobial agent. In particular, implementations of the presentinvention can be configured to efficiently and quickly provide such acoating in a rapid time period. This can enable packaging of a much moresanitary food product, including but not limited to meat primals,without hindering conventional packaging operations or speed.

For example, one exemplary implementation of packaging system includes adelivery portion with an entrance and an exit. The packaging system canfurther include a package that cooperates with the exit of the deliveryportion to receive a food item that is moved through the deliveryportion. The package has an interior surface such that an air dispenserpositioned proximate to the exit of the delivery portion. The airdispenser can at least partially inflate the package with air. Thepackaging system further can include a liquid dispenser positionedproximate to the exit of the delivery portion. The liquid dispenser canat least partially coat the interior surface of the package with asanitizing agent when the package is at least partially inflated.

Similarly, an exemplary packaging device for delivering a food item intoa package can include a staging portion configured to accept and hold afood item that is prepared for packaging. The packaging device canfurther include a delivery portion that has an entrance and an exit. Ingeneral, the food item leaves delivery portion and is delivered to apackage at or near the exit. The packaging device can also include acontroller that controls the packaging device and is communicablyconnected to a ram, an air dispenser, and a liquid dispenser. The ramcan be operatively associated with the staging portion and the deliveryportion. The ram moves the food item from the staging portion throughthe delivery portion and into the package.

Moreover, the air dispenser can be positioned proximate to the exit ofthe delivery portion and configured to at least partially inflate thepackage with air; while the liquid dispenser can be positioned proximateto the exit of the delivery portion. The air dispenser and liquiddispenser can be operatively configured to spray the sanitizing agent ina plurality of directions onto an interior surface of the package. Inone example, the controller is programmed to have the ram move the fooditem into the at least partially inflated package that has the interiorsurface at least partially coated with the sanitizing agent.

In addition to the foregoing, an exemplary method of packaging a fooditem in a sanitary package can involve inflating a package at leastpartially with air dispensed from an air dispenser. In addition, themethod can involve coating an interior surface of a package at leastpartially with a sanitizing agent dispensed from a liquid dispenser.Also, the method can involve positioning a food item within the packageby pushing the food item into the package with a ram. Furthermore, themethod can involve vacuum sealing the package around the food item.

Additional features and advantages of exemplary implementations of theinvention will be set forth in the description which follows, and inpart will be obvious from the description, or may be learned by thepractice of such exemplary implementations. The features and advantagesof such implementations may be realized and obtained by means of theinstruments and combinations particularly pointed out in the appendedclaims. These and other features will become more fully apparent fromthe following description and appended claims, or may be learned by thepractice of such exemplary implementations as set forth hereinafter.

BRIEF DESCRIPTION OF THE DRAWINGS

In order to describe the manner in which the above-recited and otheradvantages and features of the invention can be obtained, a moreparticular description of the invention briefly described above will berendered by reference to specific embodiments thereof which areillustrated in the appended drawings. Understanding that these drawingsdepict only typical embodiments of the invention and are not thereforeto be considered to be limiting of its scope, the invention will bedescribed and explained with additional specificity and detail throughthe use of the accompanying drawings in which:

FIG. 1A illustrates an example implementation of a packaging system in afirst state of an exemplary packaging process;

FIG. 1B illustrates the packaging system of FIG. 1A in a second state ofan exemplary packaging process;

FIG. 1C illustrates the packaging system of FIG. 1A in a third state ofan exemplary packaging process;

FIG. 1D illustrates the packaging system of FIG. 1A in a fourth state ofan exemplary packaging process;

FIG. 1E illustrates a top plan view of the packaging system of FIG. 1A;

FIG. 1F illustrates a bottom plan view of the packaging system of FIG.1A;

FIG. 2 illustrates a controller schematic view of an exampleimplementation of a packaging system;

FIG. 3 illustrates a graphical representation of control of a packagingsystem according to an example implementation of the present invention;and

FIG. 4 illustrates an example method of packaging a food item accordingto implementations of the present invention.

DETAILED DESCRIPTION OF SOME EXAMPLE EMBODIMENTS

The present invention extends to systems, methods and apparatusconfigured to package food items with an even coating of anantimicrobial agent. In particular, implementations of the presentinvention can be configured to efficiently and quickly provide such acoating in a rapid time period. This can enable packaging of a much moresanitary food product, including but not limited to meat primals,without hindering conventional packaging operations or speed.

Accordingly, one will appreciate from the following description andclaims that implementations of the present invention provide devices,systems, and methods that package a food item in accordance withconventional food safety standards. This allows the food items, forexample primal cuts of meat, treated in accordance with the presentinvention to avoid recall in the event of a recall relating to trimmingsand grinds. Specifically, the devices, systems and methods of packaginga food item provide a uniform coating of antimicrobial agent on the fooditem that coats the entire food item surface in a manner thateffectively protects the food from food born microbial organisms thatcan be the reason for a recall event.

To provide such advantages, at least one implementation of the presentinvention provides even application of anti-microbial agent on all sidesof the food item. In one implementation, for example, an inventivesystem/apparatus directly applies a measured, pre-determined amount ofantimicrobial solution to an inside surface of a package. When the fooditem, in turn, enters the package, the agent attaches evenly about thefood item inside the package. This type of application contrasts withcertain conventional processes that involve coating all sides of a fooditem prior to packaging, and while resting on a conveyor.

An end-user can apply agent to a food item as described herein in anautomated, efficient, and cost effective way. For instance,implementations of the present invention provide devices and systemsthat an end-user can operate to automatically control the amounts ofapplied anti-microbial agent. Such devices and systems can also controltiming and actuation of spray nozzles, as well as timed delivery of fooditem into the package. Such automated controls can ensure that almost noadditional time or labor is required to apply the antimicrobialsolution, thus making the application of antimicrobial solution a costeffective way to increase the safety of packaged food.

FIG. 1A illustrates a side view of an example implementation of apackaging system 100. In particular, FIG. 1A illustrates that thepackaging system 100 can include a staging portion 110 coupled to adelivery portion 130. FIG. 1A, in turn, shows that the delivery portioncan be operatively coupled to package 160, which ultimately receives afood item 102. Of course, one will appreciate that FIG. 1 illustratesonly one example configuration of a packaging system 100, and amanufacturer can vary the configuration from one implementation to thenext without departing from the spirit of the present invention. Forinstance, the size, shape, and operation of system 100, as well asindividual components, can vary depending on the specific application ofthe packaging system 100, or type of food item being packaged.

In particular, one will appreciate that the overall size andconfiguration of the packaging system 100 can at least somewhat dependon the type and size of a food item 102. In at least one implementation,for example, the packaging system 100 is specifically configured topackage primal cuts of beef. In other implementations, the packagingsystem 100 may be configured to package other cuts of beef, as well as(or alternatively) other meat products, such as chicken, pork, and fish.Moreover, packaging system 100 can be configured to package additionfood items 102 that are not meat products. For example, dairy products,such as cheese, and any other food item 102 that may benefit from theapplication of an antimicrobial agent, can be packaged with the packagesystem 100.

In addition to various overall configuration of the packaging system100, the material of the packaging system 100 can also vary from oneimplementation to the next. For example, a manufacturer can make thepackaging system 100 out of stainless steel (e.g., 314/316 gradestainless steel), or another food processing grade stainless steel thatresists corrosion, and that is easy to sanitize after use. Othersuitable materials may also be used depending on the nature of the fooditem 102 that a food manufacturer packages with the packaging system100.

Regardless of the packaging system 100 material, and as mentioned above,the packaging system 100 can include the staging portion 110. Amanufacturer, for example, can configure the staging portion 110 toaccept and hold the food item 102 prior to packaging thereof. Forexample, FIG. 1A shows that the packaging process may introduce the fooditem 102 into the staging portion 110 (e.g., in a form and state that issubstantially ready to be packaged). As understood more fully herein,the staging portion 110, in turn, can momentarily hold the food item 102until an operator engages ram 116.

FIG. 1A also illustrates that the staging portion 110 can include amounting bracket 118 that holds the staging portion 110, and thus thepackaging system 100, to a support (see FIG. 2). For example, FIG. 1Aillustrates an implementation of a mounting bracket 118, which caninclude a plurality of fastener ports. The end user, in turn, can inserta variety of fasteners into the fastener ports to couple the mountingbracket 118 to the support. For example, an end user can use bolts,screws, washers, and other fasteners to couple the mounting bracket tothe fixture.

In one example implementation, a manufacturer can design the mountingbracket 118 such that the position of the staging portion 110 (and thusthe position of the packaging system 100) is customizable. In oneimplementation, for example, the interface between the mounting bracket118 and the staging portion 110 can include additional hardware (notshown) that can allow a operator of the packaging system 100 to raise orlower the packaging system 100. Such hardware can also allow for anincline and/or rotation of the packaging system 100. Thus, an operatorcan customize the position of the packaging system 100 to provide a safeand comfortable operating position of the packaging system 100 while inuse.

In addition to having a customizable position, the configuration of thestaging portion 110 can vary from one implementation to the next. Forexample, FIG. 1A illustrates one example implementation where thestaging portion 110 can include a platform 112 that is surrounded by aside wall 114 to form a cavity or box-type configuration. The side wall114 can provide a boundary maintains the food item's position. In oneimplementation, a manufacturer can employ a conveyer system above oradjacent to the platform 112 such that the conveyer system canautomatically place the food item 102 in the staging area 110.Alternatively, an operator can manually deposit or position the fooditem 102 on the platform 112 within the staging area 110.

Although the platform 112 and side wall 114 illustrated in FIG. 1A havea box-type configuration, the configuration of the platform 112 and sidewall 114 can vary. For example, the platform 112 and side wall 114 canhave a more specific configuration or shape that assists in positioningthe food item 102 prior to packaging. For example, as with deliveryportion, stating portion 110 can comprise other forms such as conical ortriangular shapes. Moreover, a manufacturer can vary the size of theplatform 112 and side wall 114 such that only a predetermined volume orweight of food item 102 may be placed on the platform 112. In oneimplementation, a manufacturer can even exclude the staging portion 110from the packaging system 100, depending on the method of introducingthe food item 102 to the packaging system 100.

In addition to providing a staging area 110, the platform 112 can coupleor rest upon a weighing device, such as a scale (not shown). The scalecan communicate the weight of the food item 102 to a controller 210 (aswill be discussed in greater detail with respect to FIG. 2). This weightdetermination can allow a controller to automatically determine theamount of sanitizing agent, or antimicrobial agent, to be applied to theinterior surface of the package 160. For example, the controller can usea known density of the food item 102 and the weight of the food item 102to approximate the surface area of the food item, and thus calculate anappropriate amount of sanitizing agent to apply.

In order to move the food item 102 from the staging portion 110 andthrough the packaging system 100, a manufacturer can operativelyassociate a ram 116 with the staging portion 110. FIG. 1A illustratesthat a manufacturer can position the ram 116 to extend through the sidewall 114 of the staging area, and to move the food item 102 across theplatform 112 and through the delivery portion 130. For example, FIG. 1Aillustrates the ram 116 in a retracted position prior to pushing thefood item 102. FIG. 1C, on the other hand, illustrates the ram 116 in anextended position after having pushed the food item 102 through thedelivery portion 130.

In additional implementations, a manufacturer can employ other devicesor means to move the food item 102 into delivery portion 130 (and intothe package 160). For example, a manufacturer can incline oralternatively position platform 112 so that the food item slides, orotherwise “drops” into the package 160. Still further, the manufacturercan include a conveyor belt that conveys (rather than pushes with ram116) the food item 112 into delivery portion 130/package 160.

Even when using the illustrated ram 116, one will appreciate that amanufacturer can employ several types and configurations thereof. Forexample, the ram 116 can have a substantially cylindrical configuration.Alternatively, the ram 116 may be square, rectangular, or even pyramidalin dimension. In one implementation, the ram 116 configuration, incombination with the configuration of the delivery portion 130, can atleast partially shape the food item to a desired shape during delivery.

In addition to the various configurations of the ram 116, a manufacturercan actuate the ram 116 using a variety of different devices. In oneexample, the ram 116 is coupled to a pneumatic actuator. In thisexample, a manufacturer can configure the pneumatic actuator to move theram 116 towards the food item 102 with sufficient force and velocity toeffectively push the food item 102 in a matter of no more than about 1-2seconds. In other implementations, the ram 116 can be associated with anelectric actuator, hydraulic actuator, spring loaded actuator, or anyother similar means to provide a similar effect.

Notwithstanding the configuration of the ram 116, exampleimplementations of the packaging system 100 further include variousconfigurations of the delivery portion 130. As illustrated in FIGS. 1Athrough 1E, the delivery portion 130 can include an entrance 132 and anexit 134. The entrance 132 and the exit 134, in turn, can be configuredand sized with relation to one another such that the overallconfiguration of the delivery portion 130 has a snout-likeconfiguration. This snout-like configuration can pivot or adjust as thefood item 102 passes therethrough.

One will appreciate that various aspects of the snout-like deliveryportion 130 enable efficient coupling with package 160, and delivery ofthe food item 102. For example, FIG. 1A shows that exit 134 fits easilywithin the opening 162 of package 160. In addition, FIG. 1A shows that atop portion 136 and a bottom portion 138 of delivery portion 130 areconnected via a hinged connection 142. The hinged connection 142, inturn, allows exit 134 to have a variable cross-sectional dimension, asthe top portion 136 is allowed to rotate away from the bottom portion138. Accordingly, exit 134 can increase in size inside package 160 whenthe ram 116 pushes the food item 102 through the delivery portion 130.

In alternative implementations of the delivery portion 130, for example,a manufacturer can couple both the top portion 136 and the bottomportion 138 to the base 140 with a hinged connection, such that both thetop portion 136 and the bottom portion 138 can move with respect to oneanother. In yet an additional implementation, the manufacturer canconfigure the exit 134 of the delivery portion 130 to have a fixedcross-sectional dimension, such that the delivery portion 130 onlyallows a maximum sized food item 102 to pass through the exit 130. Inone implementation, the exit 134 can further include trim blades (notshown) that can be used to cut away the portions of the food item 102that exceed the maximum size.

Regardless of the specific delivery portion 130 and exit 134configuration, a manufacturer generally can configure the deliveryportion 130 to cooperate with one or more specific configurations of thepackage 160. For example FIG. 1A illustrates that the package 160includes an opening 162, and is made from a flexible material (e.g.,plastic) that can take the shape or form of the food item 102. Inalternative implementations, the package 160 can be made from a varietyof materials that form virtually any size and configuration.

In one example implementation, the package 160 includes properties andfeatures that allow a food manufacturer to vacuum seal the package afterthe packaging system 100 places the food item 102 within the package160. During the vacuum sealing process, all or substantially all of theair is removed from the package 160 such that the package 160 collapsestightly around the food item 102. This in turn causes the package 160 tosubstantially take the form of the food item 102. A food manufacturercan then seal the opening 162 of the package such that the package 160remains substantially formed around the food time 102 during shipment oruntil a consumer opens the package 160.

Regardless of the shape and configuration of the package 160, amanufacturer can configure the delivery portion 130 to deliver apredetermined, accurate, and substantially uniform amount of anantimicrobial agent to the interior surface of the package 160. This canbe delivered just prior to, or at substantially the same time as, thefood item 102 leaves the exit 134 of the delivery portion 130 and entersthe package 160 (See FIGS. 1B and 1C). In one example implementation,the packaging system 100 prepares the package 160 by insuring that theinterior surface of the package 160 is substantially exposed (i.e., thepackage 160 is not folded or overlapping itself). The packaging system100 then delivers an accurate and substantially uniform amount of theantimicrobial agent to the exposed interior surface of the package 160.

In order to achieve a substantially exposed interior surface of thepackage 160, the delivery portion 130 can include an air dispenser 150that can fill or otherwise inflate the package 160 with air just priorto the food item 102 leaving the exit 134 of the delivery portion 130and entering the package 160. For example, FIG. 1A illustrates animplementation in which a manufacturer has positioned air dispenser 150on the bottom portion 138 of the delivery portion 130, such that the airdispenser 150 directs air toward the interior surface of the package160. Thus, a manufacturer can configure the air dispenser 150 to inflatethe package 160 with air from the air dispenser 150. As such, theinterior surface of the package 160 is substantially exposed (i.e., thepackage 160 is not folded or overlapping itself).

In one example implementation, the air dispenser 150 comprises one ormore nozzles. The one or more nozzles, in turn, can have the ability toprovide a variety of air flow patterns into the package 160. Forexample, at least one air nozzle can provide a wide air flow patternsuch that the package 160 quickly fills with air. In otherimplementations, the air flow pattern can be narrower, depending on thesize and configuration of the package 160. In an alternativeimplementation, the air dispenser 150 can include a fixed nozzle, and/ora variable or rotatable nozzle.

Moreover, just as a nozzle on the air dispenser 150 can vary the airflow pattern, the nozzle can also vary the volume flow rate of the air.For example, a manufacturer can set a combination of air flow patternand volume flow rate to inflate package 160 in a range of about 0.1 toabout 1.5 seconds. The volume flow rate can also be adjusted accordingto the desired inflation rate of the package 160.

Another way in which the inflation rate of the package 160 can beadjusted is based on the number and/or location of the air dispenser(s).For example, FIG. 1A illustrates the packaging system 100 includes asingle air dispenser 150 on the bottom portion 138 of the deliveryportion 130. In alternative implementations, the packaging system 100include a plurality of air dispensers and/or corresponding nozzles onvarious locations of the delivery portion 130, including not only thebottom portion 138, but also the top portion 136. Furthermore, amanufacturer can direct or aim the air dispenser(s) in a variety ofdirections such that the package 160 is inflated at a rate and mannerthat allows substantially the entire interior surface of the package tobe exposed.

Once the package 160 is inflated with the air dispenser 150, thepackaging system 100 can include liquid dispenser(s) 152 that apply theantimicrobial agent to the interior surface of the package 160. Forexample, FIGS. 1A through 1B show that the delivery portion 130 caninclude an upper liquid dispenser 152 and a lower liquid dispenser 154.In one example embodiment, as illustrated in FIGS. 1A through 1F, thelower liquid dispenser 154 and the upper liquid dispenser 152 cancomprise a header with a plurality of ports 156 or nozzles through whichthe antimicrobial agent is released into the package 160.

Of course, one can appreciate that FIGS. 1A through 1D only illustrateone example configuration with respect to the upper liquid dispenser 152and the lower liquid dispenser 154. For example, the upper liquiddispenser 152 and the lower liquid dispenser 154 can alternatively havean adjustable nozzle configuration. Furthermore, the lower liquiddispenser 154 can have a header configuration while the upper liquiddispenser 152 has a nozzle configuration. Moreover, the upper liquiddispenser 152 and the lower liquid dispenser 154 can each include acombination of nozzle and header elements. In short, the upper liquiddispenser 152 and the lower liquid dispenser 154 can have variousconfigurations, spray patterns, flow rates, positions, and direction ofspray to provide an even and uniform coating of antimicrobial agent onthe interior surface of the package 160.

FIGS. 1E and 1F illustrate top and bottom plan views of the deliveryportion 130, respectively, to show further details of the upper liquiddispenser 152 and the lower liquid dispenser 154. In particular, FIG. 1Eillustrates that a manufacturer can position the upper liquid dispenser152 along the sides of the top portion 136 of the delivery portion 130.Depending on the configuration of the package 160, a manufacturer canposition the upper liquid dispenser 152 in almost any location on thetop portion 136 of the delivery portion 130.

Similarly, FIG. 1F illustrates that a manufacturer can position thelower liquid dispenser 154 in a substantially central location on thebottom portion 138 of the delivery portion 130. Just like the upperliquid dispenser 152, however, a manufacturer can position the lowerliquid dispenser 154 in virtually any location on the bottom portion 138of the delivery portion 130. In some implementations, depending on thesize and configuration of the package, a manufacturer can use only oneof the upper liquid dispenser 152 or lower liquid dispenser, as long asthe single liquid dispenser can evenly apply the antimicrobial agent tothe interior surface of the package 160.

In addition to the location of the upper and lower liquid dispensers 152and 154, FIGS. 1E and 1F illustrate the number and location of the ports156/nozzles within the header configuration of the liquid dispensers. Inparticular, FIG. 1E illustrates that the upper liquid dispenser caninclude three ports per side, while the lower liquid dispenser 154 caninclude two ports per side. In additional implementations, the upper andlower liquid dispensers 152 and 154 can include more or fewer ports 156,depending on the size and configuration of the package 160, for example.

Notwithstanding the number of ports 156, a manufacturer can configurethe ports 156 to have various sizes, directions, flow rates, and spraypatterns. For example, each port 156 included on the upper or lowerliquid dispensers 152 and 154 can be directed in a particular directionwith a specific spray pattern and flow rate. The spray pattern and flowrate can be optimized provide uniform coverage of the interior surfaceof the package 160 with agent.

The following references FIGS. 1A through 1D in sequence for oneparticular implementation of the operation of the packaging system 100.For example, FIG. 1A illustrates a first step of using the packingsystem 100 in which package 160 has been positioned around the exit 134of the delivery portion 130. In addition, FIG. 1A shows that a food item102 has been positioned in the staging area 110. As previouslydiscussed, the position of package 160 and food item 102 can be donemanually or automatically.

For example, another piece of food processing equipment, such as aconveyer system (not shown), may have automatically loaded the food item102 onto the platform 112. Likewise, a machine or similar automateddevice can position the package 160 around the exit 134 of the deliveryportion 130. In additional or alternative implementations, an operatorsimply can use their hands to slide the package 160 over the exit 134 ofthe delivery portion 130.

FIG. 1B illustrates a second step in which the packaging system 100inflates the package 160 in preparation of the application of theantimicrobial agent. In particular, FIG. 1B illustrates that airdispenser 150 dispenses an air spray 164 into the package 160 to atleast partially inflate the package 160. In one implementation, the airspray 164 completely inflates the package 160. In order to properlyinflate the package 160, the air dispenser 150 may be set to dispensethe air spray 164 for a pre-determined amount of time. For example, theair dispenser 150 may be configured to dispense the air spray 164 for anamount of time within the range of about 0.1 seconds to about 1.5seconds. An operator can user longer or shorter dispensing times,depending on the size of the package 160.

FIG. 1C illustrates the packaging system 100 in an example third step.In particular, once the package 160 is inflated, the upper liquiddispenser 152 and the lower liquid dispenser 154 can dispense a liquidspray 166 to the interior surface of the package 160. For example, FIG.1C illustrates an implementation in which an operator programs the airdispenser 150 and the lower and upper liquid dispensers 152 and 154 toactivate during the same period of time. Of course, one will appreciatethat an operator can alternatively activate the air and liquiddispensers during different periods of time, or during partiallyoverlapping periods of time.

As discussed with respect to the air dispenser 150, the upper liquiddispenser 152 and the lower liquid dispenser 154 can spray apredetermined amount of liquid spray 166 to ensure uniform distribution.The amount of liquid, or antimicrobial agent, dispensed can becontrolled by the flow rate, as well as the amount of time the upperliquid dispenser 152 and the lower liquid dispenser 154 dispense theliquid spray 166. The amount of liquid needed depends on the package 160size as well as the size and type of the food item 102.

In addition, FIG. 1C shows that just before, during, or just after theliquid dispensers are applying the liquid spray 166 to the package 160,the ram 116 is actuated and moves the food item 102 from the platform112, through the entrance 132 of the delivery portion 130 and toward theexit 134 of the delivery portion 130. In one implementation, the ram 116actuation is timed and coordinated with the liquid dispensers 152 and154, such that the food item 102 is positioned in the delivery portion130 during dispensing of the liquid spray 166. Thus, the upper liquiddispenser 152 and the lower liquid dispenser 154 can have a consistentspray pattern from one packaging cycle to the next without the food item102 interrupting or blocking the liquid spray 166.

Once the food item 102 begins to move through the exit 134 of thedelivery portion 130, however, the liquid dispensers 152 and 154 ceasedispensing additional liquid, shown in FIG. 1D as an example fourthstep. The food item 102 then moves completely into the package 160.After the food packaging system 100 positions the food item 102 withinthe package 160, the operator can then seal the package 160.

In one implementation, an operator can vacuum seal the package 160 withthe food item 102 inside the package 160. In this implementation, thevacuum sealing process collapses the package 160 tightly around the fooditem 102, such that the antimicrobial agent applied to the interiorsurface of the package 160 comes into contact with the food item 102. Inparticular, the vacuum sealing process causes further even distributionof the anti-bacterial agent around the food item 102 as the air isremoved from the package 160 and the anti-bacterial agent is evenlypressed between the package 160 and all surfaces of the food item 102.

FIG. 2 illustrates is a schematic diagram showing additional componentsand systems that can be used in conjunction with the packaging system100. For example, and as previously discussed, FIG. 2 shows variouscomponents and systems that can assist in providing control over the airdispenser 150 and the upper and lower liquid dispensers 152 and 154. Inparticular, FIG. 2 illustrates that the packaging system 100 can includea main liquid line 200 and a main air line 202. The main liquid line 200and the main air line 202 are connected to a liquid supply and airsupply, respectively.

Each of the main liquid line 200 and main air line 202 can furtherinclude pressure transducers 204 that monitor the pressure in the mainliquid line 200 and the main air line 202. FIG. 2 illustrates that thepressure transducers 204 can communicably connect to a controller 210,such that the controller receives pressure feedback from the main liquidline 200 and the main air line 202. In one implementation, when thepressure in either the main liquid line 200 or the main air line 202drops below a predetermined pressure, or rises above a predeterminedpressure, the controller can shut the packaging system 100 down andproduce a corresponding error signal.

In addition to the pressure transducers 204, the main liquid line 200and the main air line 202 can further include one or more pressuregauges 206. The one or more pressure gauges 206 can allow an operatorcan physically inspect the pressure at a certain point in the mainliquid line 200 or the main air line 202. For example, FIG. 2illustrates that the main liquid line 200 includes two pressure gauges206, such that an operator can physically inspect the pressure at apoint in the line before a filter 208, and after the filter 208.Although not shown, the main air line 202 can also include more than onepressure gauge 206 and filter 208.

Additionally, the main liquid line 200 and the main air line 202 caninclude pressure regulators 212 to regulate the pressure that the willbe supplied to the air dispenser 150 and liquid dispensers 152 and 154.In one implementation, the pressure regulators 212 can communicablyconnect to the controller 210. In such an implementation, the controller210 can control the pressure that is supplied to the air dispenser 150and the liquid dispensers 152 and 154.

Moreover, the main liquid line 200 and the main air line 202 can connectto a flow control manifold 216 that can control the flow rate throughthe main liquid line 200 and main air line 202. As with the pressureregulators 212, the flow control manifold 216 can communicably connectto the controller 210 (not shown), such that the controller can controlthe flow rate through the main liquid line 200 and the main air line202. Alternatively, an operator can manually set the flow controlmanifold 216 to provide a constant flow rate through the main liquidline 200 and the main air line 202.

FIG. 2 further illustrates that the main liquid line 200 and the mainair line 202 can include one or more electrically activated valves 214.In an exemplary implementation, the electrically activated valves 214can be solenoid valves that open and close based on a signal from thecontroller 200. In essence, the electrically activated valves 214 canprovide an on/off function to the air dispenser 150 and the liquiddispensers 152 and 154. Thus, when the electrically activated valves 214are open, the air dispenser 150 and the liquid dispensers 152 and 154dispense air and liquid, respectively. By contrast, when theelectrically activated valves 214 are closed, the air dispenser 150 andthe liquid dispensers 152 and 154 do not dispense.

Notwithstanding the illustration in FIG. 2, a manufacturer can arrangethe pressure transducer(s) 204, pressure gauge(s) 206, filter(s) 208,pressure regulator(s) 212, electrically activated valves 214, and theflow control manifold 216 in various orders and locations along the mainliquid line 200 and main air line 202. Moreover, the packaging system100 can further include additional transducers, gauges, filters,regulators, meters, and manifolds (not shown) depending on the specificapplication of the packaging system 100.

As discussed above, FIG. 2 shows that the packaging system 100 caninclude controller 210 that an operator can program to control variousfunctions of the packaging system 100. Although FIG. 2 illustrates thecontroller in a schematic, a manufacturer can mount the controller 210directly to the packaging system 100, or alternatively, the controller210 can be mounted separate from the packaging system 100. In oneexample, the controller 210 can attach to the base 140, such that anoperator can easily access the controller 210 to adjust the function ofthe packaging system 100.

One will appreciate that the controller 210 can use a combination oftimers, input and output signal monitoring, and signal generators thatare controlled by computer-executable instructions to control thepackaging system 100. For example, FIG. 2 shows that controller 210 ispositioned with one or more lines to control all or many of the abovedescribed functions of the packaging system 100, including, but notlimited to, dispensing the air spray 164, dispensing the liquid spray166, and actuating the ram 116.

In one example implementation, the controller can monitor for a cyclestart input signal. FIG. 2 illustrates that an operator can prompt thecycle start input signal input by pressing a button 220, such as a footpedal as shown in FIG. 2. In other implementations, the button 220 canbe a hand button or hip switch that provides the cycle start input tothe controller 210.

In addition (or as an alternative) to the button providing a cycle startinput to the controller 210, a package detector 218 can detect thepresence of the package 160 and signal to the controller 210 that thepackage 160 is in proper position. For example, FIG. 2 illustrates thatthe packaging system can include the package detector 218 positioned onthe exit 134 of the delivery portion 130. The package detector 218 canprovide the controller 210 with an input signal to indicate to thecontroller 210 that the package 160 is positioned properly. If thepackage 160 is not positioned properly, then the package detector 218does not provide the input signal to the controller 210, and thecontroller 210 does not allow the packaging process to continue.

In one implementation, the package detector 218 can be a sensor that candetect the presence of the package 160 about the exit 134 of thedelivery portion 130. The sensor may include a proximity sensor, a lasersensor, or any other similar sensory device that can provide an inputsignal based on the detection of the presence of the package 160.

After the controller 210 receives the cycle start input from the button220 and/or the package detect input from the package detector 218, forexample, then the controller 210 can signal to the electrical activatedvalve(s) 214 to dispense the air and/or liquid in a predeterminedmanner. Thereafter, the controller 210 can actuate a actuator 222connected to the ram 116. Upon actuation, the ram 116 pushes the fooditem 102 into the package 160 that has the interior surface coated withthe antimicrobial agent liquid. In other words, once an operatorpositions the package 160 around the exit 134 of the delivery portion130 and presses the button 220, the packaging system 100 automaticallyinflates the package 160. The packaging system 100 then applies an evencoat of antimicrobial agent to the interior surface of the package 160,and pushes the food item into the package 160.

The manner and timing in which the controller 210 controls the airdispenser 150 and the liquid dispensers 152 and 154 can vary from oneimplementation to the next. As FIG. 3 illustrates, for example, thecontroller 210 can provide that the air dispenser 150 dispense air for aperiod of X seconds (e.g., the period between the start of the cycle Sand X). The liquid dispensers 152 and 154, however, have a delay for aperiod of Y seconds (e.g., the period between S and Y). As shown in FIG.3, X is greater than Y. This means that there is a portion of time whenonly the air is dispensing (e.g., the period between S and Y), and thereis a portion of time when both the air and the liquid is dispensing(e.g., the period between Y and X).

Continuing with the example illustrated in FIG. 3, the controller 210can signal to the electrical activated valve 214 associated with theliquid dispensers to cause the liquid dispensers to have a spray outputfor Z seconds, after the delay of Y seconds. Additionally, asillustrated, after X seconds of air output, the controller 210 cansignal to the electrical activated valve 214 associated with the airdispenser 150 to cause the air dispenser 150 to stop dispensing airspray 164.

In particular, in one implementation, an operator can program thecontroller 210 such that the air dispenser 150 and the liquid dispensers152 and 154 activate during partially overlapping periods of time. Forexample, the operator can program the controller 210 such that the airdispenser 150 sprays air for a total period of about 0.5 seconds (i.e.,the period between S and X), and the liquid dispensers 152 and 154dispense the antimicrobial agent for a total period of about 0.5 seconds(i.e., the period between Y and Z). In addition, the operator maydifferentially activate air dispenser 150 and the liquid dispensers 152and 154 at the same time for only about 0.25 seconds (i.e., the periodbetween Y and X).

In particular, halfway through the 0.5 second air dispensing period, orafter about 0.25 seconds of dispensing air, the liquid dispensers 152and 154 can begin dispensing liquid. In this case, both the airdispenser 150 and the liquid dispensers 152 and 154 are activated forthe last half of the air dispensing period (about 0.25 seconds). Afterthe air dispenser 150 completes the total 0.5 second period, the liquiddispensers 152 and 154 can continue to dispense the antimicrobial agentfor about another 0.25 seconds to complete the total liquid dispensingperiod.

The example time periods of X, Y, and Z can all vary such that theperiods of overlap differ from one implementation to the next. Thisvariance can be configured depending on the size of package 160, type offood item 102, size of food item 102, and other variables that mayaffect spray times and patterns. For example, in some implementations,there is no overlap between the air dispensing and the liquiddispensing. Additionally, the air and the liquid dispensing maycompletely overlap.

Accordingly, FIGS. 1A through FIG. 3 and the corresponding text providea number of different components and systems that can efficientlypackage a food item with a predetermined amount and even coating ofantimicrobial agent. In addition to the foregoing, implementations ofthe present invention can also be described in terms of flowchartscomprising one or more acts in a method for accomplishing a particularresult. For example, FIG. 4 illustrates a method of packaging a fooditem in a sanitary package. The acts of FIG. 4 are discussed more fullybelow with respect to the components discussed with reference to FIGS.1A through FIG. 3.

For example, FIG. 4 shows that the method of packaging a food item in asanitary package can comprise an act 402 of inflating a bag with air.Act 402 includes inflating a package at least partially with an airdispenser. For example, FIG. 1B illustrates the air dispenser 150dispensing an air spray 164 to inflate the package 160.

FIG. 4 also shows that the method can comprise an act 404 of coating theinterior surface with a sanitizing agent. Act 404 includes coating aninterior surface of a package at least partially with a sanitizing agentdispensed from a liquid dispenser. For example, FIG. 1C illustrates theupper and lower liquid dispensers 152 and 154 dispending anantimicrobial agent onto the interior surface of the package 160.

In addition, FIG. 4 illustrates that the method can comprise an act 406of positioning a food item in the package. Act 406 includes positioninga food item within the package by pushing the food item into the packagewith a ram. For example, FIG. 1C and 1D illustrate that ram 116 haspushed the food item 102 into the package 160.

Furthermore, FIG. 4 illustrates that the method can comprise an act 408of collapsing the package around the food item. Act 408 includes vacuumsealing the package around the food item. For example, after the fooditem 102 is positioned within the package 160, as illustrated in FIG.1D, an operator can vacuum seal the package 160 to collapse the interiorsurface of the package 160 around the food item 102.

Accordingly, the diagrams and text corresponding to FIGS. 1A throughFIG. 4 illustrate or otherwise describe a number of methods, devices,systems, configurations, and components that an operator can use topackage a food item in a sanitary and safe package. Such methods,devices, systems, configurations, and components can provide anefficient, reliable, and repeatable packaging process when compared toconventional devices and methods. For example, and as previouslydescribed, successive food items can be individually and uniformlytreated and packaged in a matter of mere seconds, or less, per fooditem. Thus, food manufacturers can use implementations of the presentinvention to safely, reliably and efficiently package food items in asanitary package prior to shipping.

The present invention may be embodied in other specific forms withoutdeparting from its spirit or essential characteristics. The describedimplementations are to be considered in all respects only asillustrative and not restrictive. The scope of the invention is,therefore, indicated by the appended claims rather than by the foregoingdescription. All changes that come within the meaning and range ofequivalency of the claims are to be embraced within their scope.

We claim:
 1. A packaging system for packaging a food item and asanitizing agent into a package, the packaging system comprising: adelivery portion having an exit with a variable cross-sectionaldimension that operatively couples to the package to deliver the fooditem into the package as the food item moves through the exit; acontroller that receives a food item characteristic associated with thefood item and determines an amount of the sanitizing agent to apply tothe package based on the food item characteristic; an air dispensercommunicably connected to the controller and positioned proximate theexit in order to at least partially inflate the package with air; and aliquid dispenser communicably connected to the controller and positionedproximate the exit in order to dispense the amount of the sanitizingagent determined by the controller.
 2. The packaging system as recitedin claim 1, further comprising: a top portion of the delivery portionhaving a nozzle of the liquid dispenser; and a bottom portion of thedelivery portion having a header of the liquid dispenser.
 3. Thepackaging system as recited in claim 1, further comprising: a topportion of the delivery portion having a first nozzle of the liquiddispenser and a first header of the liquid dispenser; and a bottomportion of the delivery portion having a second nozzle of the liquiddispenser and a second header of the liquid dispenser.
 4. The packagingsystem as recited in claim 1, wherein the air dispenser comprises: afirst nozzle having a wide air flow pattern; and a second nozzle havinga narrow air flow pattern.
 5. The packaging system as recited in claim1, wherein the liquid dispenser comprises: a nozzle; and a header havinga plurality of ports.
 6. The packaging system as recited in claim 1,further comprising: a staging portion that cooperates with the deliveryportion, the staging portion having a platform for receiving the fooditem; a mounting bracket that holds the staging portion; and a hardwareinterface between the mounting bracket and the staging portion tofacilitate customizable positioning of the packaging system.
 7. Thepackaging system as recited in claim 6, wherein the hardware interfacefacilitates adjusting the height of the packaging system.
 8. Thepackaging system as recited in claim 6, wherein the hardware interfacefacilitates adjusting the incline of the packaging system.
 9. Thepackaging system as recited in claim 6, wherein the hardware interfacefacilitates rotating the packaging system.
 10. The packaging system asrecited in claim 1, further comprising a flow control manifoldcommunicably connected to the controller in order to control a flow rateof the sanitizing agent to the liquid dispenser.
 11. A packaging devicecomprising: a delivery portion having an exit with a variablecross-sectional dimension, the delivery portion further having: a topportion having a hinged connection; and a bottom portion having a fixedconnection; a controller that receives a food item characteristicassociated with the food item and determines, based on the food itemcharacteristic, an amount of a sanitizing agent needed to treat the fooditem; and a liquid dispenser communicably connected to the controller inorder to dispense the amount of the sanitizing agent determined by thecontroller; wherein, in response to the controller receiving the fooditem characteristic, the controller controls the liquid dispenser todispense the amount of the sanitizing agent determined by the controllerbefore the food item moves through the exit.
 12. The packaging device asrecited in claim 11, further comprising a package detector locatedproximate the exit in order to detect when the exit is within a package,wherein: the package detector sends a signal to the controller upondetecting the package; and the controller does not proceed withcontrolling the liquid dispenser to dispense the amount of thesanitizing agent determined by the controller unless the controller hasreceived the signal from the package detector.
 13. The packaging deviceas recited in claim 12, wherein the package detector comprises at leastone of a proximity sensor or a laser sensor.
 14. The packaging device asrecited in claim 11, wherein the delivery portion is inclined such thatthe food item slides through the delivery portion and out the exit. 15.The packaging device as recited in claim 11, wherein the deliveryportion is vertically oriented such that the food item drops through thedelivery portion and out the exit.
 16. A packaging device comprising: adelivery portion having an exit with a fixed cross-sectional dimension;a controller that receives a food item characteristic associated withthe food item and determines, based on the food item characteristic, anamount of a sanitizing agent needed to treat the food item; and a liquiddispenser communicably connected to the controller in order to dispensethe amount of the sanitizing agent determined by the controller;wherein, in response to the controller receiving the food itemcharacteristic, the controller controls the liquid dispenser to dispensethe amount of the sanitizing agent determined by the controller beforethe food item moves through the exit.
 17. The packaging device asrecited in claim 16, further comprising: an air dispenser communicablyconnected to the controller in order to at least partially inflate apackage; wherein the liquid dispenser dispenses the amount of thesanitizing agent determined by the controller into the package beforethe food item moves into the package.
 18. The packaging device asrecited in claim 17, further comprising a ram communicably connected tothe controller in order to move the food item through the exit and intothe package.
 19. The packaging device as recited in claim 16, furthercomprising a food item characteristic detector communicably connected tothe controller in order to send the food item characteristic associatedwith the food item to the controller.
 20. The packaging device asrecited in claim 19, wherein, based on the food item characteristicreceived by the controller, the controller determines an additional fooditem characteristic associated with the food item in order to determinethe amount of the sanitizing agent needed to treat the food item.